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Preclinical Evaluation of a Fluorescent Probe Targeting Receptor CDCP1 for Identification of Ovarian Cancer.
He, Yaowu; Khan, Tashbib; Kryza, Thomas; Jones, Martina L; Goh, Justin B; Lyons, Nicholas J; Pearce, Lesley A; Lee, Michael D; Gough, Madeline; Rogers, Rebecca; Davies, Claire M; Gilks, C Blake; Hodgkinson, Thomas; Lourie, Rohan; Barry, Sinead C; Perrin, Lewis C; Williams, Charlotte C; Puttick, Simon; Adams, Timothy E; Munro, Trent P; Hooper, John D; Chetty, Naven.
Afiliação
  • He Y; Mater Research Institute - The University of Queensland, Translational Research Institute, 37 Kent Street, Woolloongabba, QLD 4102, Australia.
  • Khan T; Mater Research Institute - The University of Queensland, Translational Research Institute, 37 Kent Street, Woolloongabba, QLD 4102, Australia.
  • Kryza T; Mater Research Institute - The University of Queensland, Translational Research Institute, 37 Kent Street, Woolloongabba, QLD 4102, Australia.
  • Jones ML; Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, QLD 4072, Australia.
  • Goh JB; Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, QLD 4072, Australia.
  • Lyons NJ; Mater Research Institute - The University of Queensland, Translational Research Institute, 37 Kent Street, Woolloongabba, QLD 4102, Australia.
  • Pearce LA; CSIRO Manufacturing, Parkville, VIC 3052, Australia.
  • Lee MD; CSIRO Manufacturing, Parkville, VIC 3052, Australia.
  • Gough M; Mater Research Institute - The University of Queensland, Translational Research Institute, 37 Kent Street, Woolloongabba, QLD 4102, Australia.
  • Rogers R; Mater Research Institute - The University of Queensland, Translational Research Institute, 37 Kent Street, Woolloongabba, QLD 4102, Australia.
  • Davies CM; Mater Health Services, South Brisbane, QLD 4101, Australia.
  • Gilks CB; Mater Research Institute - The University of Queensland, Translational Research Institute, 37 Kent Street, Woolloongabba, QLD 4102, Australia.
  • Hodgkinson T; Mater Health Services, South Brisbane, QLD 4101, Australia.
  • Lourie R; Department of Pathology and Laboratory Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, BC V6T 2B5, Canada.
  • Barry SC; Karl Storz Endoscopy, West End, QLD 4101, Australia.
  • Perrin LC; Mater Health Services, South Brisbane, QLD 4101, Australia.
  • Williams CC; Mater Health Services, South Brisbane, QLD 4101, Australia.
  • Puttick S; Mater Health Services, South Brisbane, QLD 4101, Australia.
  • Adams TE; CSIRO Manufacturing, Parkville, VIC 3052, Australia.
  • Munro TP; CSIRO Manufacturing, Parkville, VIC 3052, Australia.
  • Hooper JD; CSIRO Manufacturing, Parkville, VIC 3052, Australia.
  • Chetty N; Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, QLD 4072, Australia.
Mol Pharm ; 18(9): 3464-3474, 2021 09 06.
Article em En | MEDLINE | ID: mdl-34448393
ABSTRACT
Optimal cytoreduction for ovarian cancer is often challenging because of aggressive tumor biology and advanced stage. It is a critical issue since the extent of residual disease after surgery is the key predictor of ovarian cancer patient survival. For a limited number of cancers, fluorescence-guided surgery has emerged as an effective aid for tumor delineation and effective cytoreduction. The intravenously administered fluorescent agent, most commonly indocyanine green (ICG), accumulates preferentially in tumors, which are visualized under a fluorescent light source to aid surgery. Insufficient tumor specificity has limited the broad application of these agents in surgical oncology including for ovarian cancer. In this study, we developed a novel tumor-selective fluorescent agent by chemically linking ICG to mouse monoclonal antibody 10D7 that specifically recognizes an ovarian cancer-enriched cell surface receptor, CUB-domain-containing protein 1 (CDCP1). 10D7ICG has high affinity for purified recombinant CDCP1 and CDCP1 that is located on the surface of ovarian cancer cells in vitro and in vivo. Our results show that intravenously administered 10D7ICG accumulates preferentially in ovarian cancer, permitting visualization of xenograft tumors in mice. The data suggest CDCP1 as a rational target for tumor-specific fluorescence-guided surgery for ovarian cancer.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Moléculas de Adesão Celular / Imagem Óptica / Corantes Fluorescentes / Anticorpos Monoclonais Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Moléculas de Adesão Celular / Imagem Óptica / Corantes Fluorescentes / Anticorpos Monoclonais Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article